Usher syndrome type 1D

Term ID

DOID:0110831

Synonyms

• USH1D
• Usher syndrome type ID

Definition

An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22. https://www.ncbi.nlm.nih.gov/pubmed/11138009

References

• ICD10CM:H35.5
• OMIM:601067

Ontology

Human Disease   ( DOID:0110831 )